Remote Oncology Clinical Research Associate

Parexel; Montpelier (VT); Remote; USD 65,000 - 90,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all phases of a clinical trial. You will coordinate monitoring visits, ensure site readiness, and manage regulatory documents to ensure compliance with ICH-GCP and sponsor SOPs.

The role emphasizes building strong site relationships, conducting on-site and remote monitoring, and collaborating with sponsor roles to maintain study integrity, data quality, and patient safety.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Bachelor's degree preferred with science/biology emphasis.
• Experience with ICH-GCP and country clinical research guidelines.

Responsibilities

• Act as the primary site contact and site manager across all phases of the trial.
• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Gathers and reviews regulatory documentation for start-up, maintenance and close-out.
• Communicates with investigators and site staff on protocol conduct, recruitment and regulatory issues.

Skills

Site management

Monitoring skills

Communication

Regulatory knowledge

Data analysis

Travel readiness

ICH-GCP knowledge

Mentorship

Education

Bachelor's degree in science/biology

Tools

MS Office

Clinical Trial Management Systems

eTMF (Electronic Trial Master File)

Job description

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all phases of a clinical trial. You will coordinate monitoring visits, ensure site readiness, and manage regulatory documents to ensure compliance with ICH-GCP and sponsor SOPs.

The role emphasizes building strong site relationships, conducting on-site and remote monitoring, and collaborating with sponsor roles to maintain study integrity, data quality, and patient safety.